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I V Flow Regulator. - India CDSCO Medical Device Registration

I V Flow Regulator. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000033_9a4689c92af9d6c1e146a8ec4b5d24ea_9ac3316066de5b311fd524709434fac7. This device is marketed under the brand name VIGGO-MANIFOLD-2WAY & VIGGO-MANIFOLD-3WAY. The license holder is Viggo Medical Devices India Private Limited, and it is classified as Device Class Class B. The approving authority is Haryana.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
I V Flow Regulator.
UID: MFG/MD/2021/000033_9a4689c92af9d6c1e146a8ec4b5d24ea_9ac3316066de5b311fd524709434fac7

Brand Name

VIGGO-MANIFOLD-2WAY & VIGGO-MANIFOLD-3WAY

Device Class

Class B

Approving Authority

Haryana

Product Information

An IV system and administration device offering precision care and consistent delivery

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